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Investigation of brain iron levels in Chinese patients with Alzheimer’s disease

INTRODUCTION: We aimed (i) to explore the diagnostic value of deep gray matter magnetic susceptibility in Alzheimer’s disease (AD) in China and (ii) to analyze its correlation with neuropsychiatric scales. Moreover, we conducted subgroup analysis based on the presence of the APOE-ε4 gene to improve...

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Autores principales: Huang, Chuanbin, Li, Jing, Liu, Chang, Zhang, Yong, Tang, Qiqiang, Lv, Xinyi, Ruan, Mengyue, Deng, Kexue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10239950/
https://www.ncbi.nlm.nih.gov/pubmed/37284016
http://dx.doi.org/10.3389/fnagi.2023.1168845
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author Huang, Chuanbin
Li, Jing
Liu, Chang
Zhang, Yong
Tang, Qiqiang
Lv, Xinyi
Ruan, Mengyue
Deng, Kexue
author_facet Huang, Chuanbin
Li, Jing
Liu, Chang
Zhang, Yong
Tang, Qiqiang
Lv, Xinyi
Ruan, Mengyue
Deng, Kexue
author_sort Huang, Chuanbin
collection PubMed
description INTRODUCTION: We aimed (i) to explore the diagnostic value of deep gray matter magnetic susceptibility in Alzheimer’s disease (AD) in China and (ii) to analyze its correlation with neuropsychiatric scales. Moreover, we conducted subgroup analysis based on the presence of the APOE-ε4 gene to improve the diagnosis of AD. METHODS: From the prospective studies of the China Aging and Neurodegenerative Initiative (CANDI), a total of 93 subjects who could undergo complete quantitative magnetic susceptibility imaging and APOE-ε4 gene detection were selected. Differences in quantitative susceptibility mapping (QSM) values between and within groups, including AD patients, individuals with mild cognitive impairment (MCI), and healthy controls (HCs), both APOE-ε4 carriers and non-carriers, were analyzed. RESULTS: In primary analysis, the magnetic susceptibility values of the bilateral caudate nucleus and right putamen in the AD group and of the right caudate nucleus in the MCI group were significantly higher than those in the HCs group (P < 0.05). In APOE-ε4 non-carriers, there were significant differences in more regions between the AD, MCI, and HCs groups, such as the left putamen and the right globus pallidus (P < 0.05). In subgroup analysis, the correlation between QSM values in some brain regions and neuropsychiatric scales was even stronger. DISCUSSION: Exploration of the correlation between deep gray matter iron levels and AD may provide insight into the pathogenesis of AD and facilitate early diagnosis in elderly Chinese. Further subgroup analysis based on the presence of the APOE-ε4 gene may further improve the diagnostic efficiency and sensitivity.
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spelling pubmed-102399502023-06-06 Investigation of brain iron levels in Chinese patients with Alzheimer’s disease Huang, Chuanbin Li, Jing Liu, Chang Zhang, Yong Tang, Qiqiang Lv, Xinyi Ruan, Mengyue Deng, Kexue Front Aging Neurosci Neuroscience INTRODUCTION: We aimed (i) to explore the diagnostic value of deep gray matter magnetic susceptibility in Alzheimer’s disease (AD) in China and (ii) to analyze its correlation with neuropsychiatric scales. Moreover, we conducted subgroup analysis based on the presence of the APOE-ε4 gene to improve the diagnosis of AD. METHODS: From the prospective studies of the China Aging and Neurodegenerative Initiative (CANDI), a total of 93 subjects who could undergo complete quantitative magnetic susceptibility imaging and APOE-ε4 gene detection were selected. Differences in quantitative susceptibility mapping (QSM) values between and within groups, including AD patients, individuals with mild cognitive impairment (MCI), and healthy controls (HCs), both APOE-ε4 carriers and non-carriers, were analyzed. RESULTS: In primary analysis, the magnetic susceptibility values of the bilateral caudate nucleus and right putamen in the AD group and of the right caudate nucleus in the MCI group were significantly higher than those in the HCs group (P < 0.05). In APOE-ε4 non-carriers, there were significant differences in more regions between the AD, MCI, and HCs groups, such as the left putamen and the right globus pallidus (P < 0.05). In subgroup analysis, the correlation between QSM values in some brain regions and neuropsychiatric scales was even stronger. DISCUSSION: Exploration of the correlation between deep gray matter iron levels and AD may provide insight into the pathogenesis of AD and facilitate early diagnosis in elderly Chinese. Further subgroup analysis based on the presence of the APOE-ε4 gene may further improve the diagnostic efficiency and sensitivity. Frontiers Media S.A. 2023-05-22 /pmc/articles/PMC10239950/ /pubmed/37284016 http://dx.doi.org/10.3389/fnagi.2023.1168845 Text en Copyright © 2023 Huang, Li, Liu, Zhang, Tang, Lv, Ruan and Deng. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Huang, Chuanbin
Li, Jing
Liu, Chang
Zhang, Yong
Tang, Qiqiang
Lv, Xinyi
Ruan, Mengyue
Deng, Kexue
Investigation of brain iron levels in Chinese patients with Alzheimer’s disease
title Investigation of brain iron levels in Chinese patients with Alzheimer’s disease
title_full Investigation of brain iron levels in Chinese patients with Alzheimer’s disease
title_fullStr Investigation of brain iron levels in Chinese patients with Alzheimer’s disease
title_full_unstemmed Investigation of brain iron levels in Chinese patients with Alzheimer’s disease
title_short Investigation of brain iron levels in Chinese patients with Alzheimer’s disease
title_sort investigation of brain iron levels in chinese patients with alzheimer’s disease
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10239950/
https://www.ncbi.nlm.nih.gov/pubmed/37284016
http://dx.doi.org/10.3389/fnagi.2023.1168845
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